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Interactive Learning Environments, ISSN 1049-4820, 06/2014, Volume 24, Issue 6, pp. 1076 - 1096
Journal Article
META: tijdschrift voor bibliotheek & archief, ISSN 2033-639X, 01/2013, Volume 89, Issue 9, pp. 30 - 30
The New York Times christened 2012 as 'The Year of the MOOC.' Since then MOOCs, are fully Massive Open Online Courses, many top trend list. A MOOC is a form of... 
Journal Article
Journal Article
Journal of Social Science Education, 03/2016, Volume 15, Issue 1
This article presents the findings of a qualitative study (carried out between 2011 and 2013) about the adoption and implementation of learning paths within a... 
Journal Article
Journal of Social Science Education, 03/2016, Volume 15, Issue 1, pp. 27 - 37
This article presents the findings of a qualitative study (carried out between 2011 and 2013) about the adoption and implementation of learning paths within a... 
Journal Article
Proceedings of the European Conference on Games-based Learning, ISSN 2049-0992, 2018, Volume 2018-, pp. 549 - 555
Conference Proceeding
JBR-BTR, ISSN 1780-2393, 2015, Volume 99, Issue 2, pp. 43 - 46
Congenital esophageal stenosis due to tracheobronchial remnants is defined as an intrinsic stenosis of the esophagus caused by congenital architectural... 
Esophageal stenosis | Infant | Constriction | Duodenal obstruction | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | RING | Esophageal stenosis, Constriction, Duodenal obstruction, Infant
Journal Article
Molecular Imaging and Biology, ISSN 1536-1632, 12/2016, Volume 18, Issue 6, pp. 887 - 897
Gelsolin amyloidosis (AGel), also known as familial amyloidosis, Finnish type (FAF), is an autosomal, dominant, incurable disease caused by a point mutation... 
Nanobody | AGel | Medicine & Public Health | VHH | Gelsolin | Imaging / Radiology | SPECT
Journal Article
Molecular Imaging and Biology : MIB, ISSN 1536-1632, 12/2016, Volume 18, Issue 6, p. 887
Purpose Gelsolin amyloidosis (AGel), also known as familial amyloidosis, Finnish type (FAF), is an autosomal, dominant, incurable disease caused by a point... 
Journal Article
Molecular Imaging and Biology, ISSN 1536-1632, 12/2016, Volume 18, Issue 6, pp. 887 - 897
Gelsolin amyloidosis (AGel), also known as familial amyloidosis, Finnish type (FAF), is an autosomal, dominant, incurable disease caused by a point mutation... 
Journal Article
Molecular Imaging and Biology, ISSN 1536-1632, 12/2016, Volume 18, Issue 6, p. 887
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s11307-016-0960-y... 
CT imaging | Peptides | Gene mutations | SPECT imaging | Amyloidosis
Journal Article
AIDS Research and Human Retroviruses, ISSN 0889-2229, 10/2018, Volume 34, Issue S1, pp. 1 - 407
Journal Article
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